ClearanceBrief
510(k) K952029 ยท FEN Device, Cystometric, Hydraulic

RUSCH INTERNATIONAL URODYNAMIC CATHETERS

ApplicantRusch Intl., Jeffrey NH, US
DecisionSubstantially Equivalent, Jun 13, 1995
ReceivedMay 1, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952029

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.